Meshikhes Abdul-Wahed N, Al-Abkari Hussain A, Al-Momen Sami A, Saad Feryal E
Department of Surgery, Dammam Central Hospital, Dammam, Eastern Province, Kingdom of Saudi Arabia.
Saudi Med J. 2006 Mar;27(3):389-91.
Pseudomyxoma peritonei is very rare, and its exact pathogenesis is unknown. It is characterized by intra-abdominal extracellular gelatinous fluid collections. We report a case of pseudomyxoma peritonei in a 38-year-old Saudi male who presented with right iliac fossa mass and weight loss. He was treated initially as an appendicular mass and computed tomography was helpful in making the diagnosis. He was treated by laparotomy, right hemicolectomy and omentectomy, but no perioperative intraperitoneal chemotherapy was instilled. He received postoperative chemotherapy and remained alive with no recurrence at 18-month follow-up.
腹膜假黏液瘤非常罕见,其确切发病机制尚不清楚。它的特征是腹腔内出现细胞外胶冻样液体聚集。我们报告一例38岁沙特男性腹膜假黏液瘤病例,该患者表现为右下腹包块和体重减轻。他最初被当作阑尾包块治疗,计算机断层扫描有助于做出诊断。他接受了剖腹手术、右半结肠切除术和大网膜切除术,但未进行围手术期腹腔内化疗。他接受了术后化疗,在18个月的随访中存活且无复发。